We are among the world leaders in Suppositories and Pessaries dosage forms with one of the largest portfolios in this segment. Our thirty years of experience in suppositories manufacturing has resulted in developing an extensive product offering in suppositories and pessaries across various therapeutic categories (see here ). We follow European GMP Standards for manufacturing suppositories. Our manufacturing plants are certified to be cGMP compliant by local and international standards: EU GMP, WHO GMP, OHSAS-18001 : 2007 and ISO-14001 : 2004. We are the only EU-GMP certified suppositories manufacturer in India. We are constantly looking to raise the bar in terms of developing innovative products and quality standards which keep us ahead of competition in this dosage form.
Vacancy Details
Department : R&D Analytical Development
Designation Research Associate/ Senior Research Associate
Qualification : M.Sc. /M. Pharm
Experience: 3-8 Yrs.
Job profiles:
• Perform activities of analytical development strategy and execute its
implementation to meet the timeline
• Perform analytical method development, analysis of trial samples and method
transfer activities as per procedures and completion of same within the time
frame to meet the timeline.
• Perform analysis and laboratory activities as per SOPs to ensure compliance.
• Study and discuss with team lead for technical guidance and evaluate self-
performance to ensure team development and improved lab efficiency
Interested candidates can email their profile to antara.sawant@blissgvs.com
On or before 17th January 2022 with subject line “Application for Analytical”
Virtual interviews are schedule on 18th January 2022 between 4 PM to 8 PM
